How can pharmaceutical companies ensure that patients are actively involved at every stage ofdrug development? Last week I attended the Patient Centricity & Engagement conference in London to find out […]
Thanks so much to everyone for getting involved with this year’s Rare Disease Day! It’s been amazing how many of you have shown your stripes and they all look fantastic! […]
Happy Rare Disease Day! We can finally reveal the special segment recorded with Medscape for Rare Disease Day. We would like to thank everyone involved in making this happen, it […]
With my head hung down, trying to hide my morning face away from the scurry of staff hurrying between the shift changeover, I scan the floor for those familiar patterns; […]
On Tuesday Lucy was invited to present alongside Sioned Preece at the UK Astrazeneca conference held at the Intercontinental right next to the O2 in North Greenwich! Astrazeneca has recently […]
by Dr Alexandra Downes, Paediatric Registrar My Rare Disease journey began in the second year of my Human Genetics degree at University College London. I still remember to this day […]
Dr Lauren Ferretti is a paediatric registrar in London with a life-long commitment to charity fundraising and an interest in genetics and whole genome sequencing. Through working with M4RD as […]
We are M4RD and we #daretothinkrare Medics4RareDiseases is a registered charity started by medics, for medics! In fact, M4RD started out as a university society at Barts & The London. […]
Medics4RareDiseases has been accredited as a Living Wage Employer. Our Living Wage commitment will see everyone working at M4RD receive a minimum hourly wage of £9.90 in the UK or […]
Agata Oliwa has recently finished her medical degree at the University of Glasgow. She has started the Specialist Academic Foundation Programme this summer in the North East. Agata aspires to […]